IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v12y2021i1d10.1038_s41467-021-27422-1.html
   My bibliography  Save this article

Acute RyR1 Ca2+ leak enhances NADH-linked mitochondrial respiratory capacity

Author

Listed:
  • Nadège Zanou

    (University of Lausanne)

  • Haikel Dridi

    (Columbia University Vagelos College of Physicians and Surgeons)

  • Steven Reiken

    (Columbia University Vagelos College of Physicians and Surgeons)

  • Tanes Imamura de Lima

    (École Polytechnique Fédérale de Lausanne (EPFL))

  • Chris Donnelly

    (University of Lausanne)

  • Umberto De Marchi

    (Nestlé Research – École Polytechnique Fédérale de Lausanne (EPFL))

  • Manuele Ferrini

    (University of Lausanne)

  • Jeremy Vidal

    (University of Lausanne)

  • Leah Sittenfeld

    (Columbia University Vagelos College of Physicians and Surgeons)

  • Jerome N. Feige

    (Nestlé Research – École Polytechnique Fédérale de Lausanne (EPFL)
    École Polytechnique Fédérale de Lausanne (EPFL))

  • Pablo M. Garcia-Roves

    (L’Hospitalet del Llobregat)

  • Isabel C. Lopez-Mejia

    (University of Lausanne)

  • Andrew R. Marks

    (Columbia University Vagelos College of Physicians and Surgeons
    Columbia University Medical Center)

  • Johan Auwerx

    (École Polytechnique Fédérale de Lausanne (EPFL))

  • Bengt Kayser

    (University of Lausanne)

  • Nicolas Place

    (University of Lausanne)

Abstract

Sustained ryanodine receptor (RyR) Ca2+ leak is associated with pathological conditions such as heart failure or skeletal muscle weakness. We report that a single session of sprint interval training (SIT), but not of moderate intensity continuous training (MICT), triggers RyR1 protein oxidation and nitrosylation leading to calstabin1 dissociation in healthy human muscle and in in vitro SIT models (simulated SIT or S-SIT). This is accompanied by decreased sarcoplasmic reticulum Ca2+ content, increased levels of mitochondrial oxidative phosphorylation proteins, supercomplex formation and enhanced NADH-linked mitochondrial respiratory capacity. Mechanistically, (S-)SIT increases mitochondrial Ca2+ uptake in mouse myotubes and muscle fibres, and decreases pyruvate dehydrogenase phosphorylation in human muscle and mouse myotubes. Countering Ca2+ leak or preventing mitochondrial Ca2+ uptake blunts S-SIT-induced adaptations, a result supported by proteomic analyses. Here we show that triggering acute transient Ca2+ leak through RyR1 in healthy muscle may contribute to the multiple health promoting benefits of exercise.

Suggested Citation

  • Nadège Zanou & Haikel Dridi & Steven Reiken & Tanes Imamura de Lima & Chris Donnelly & Umberto De Marchi & Manuele Ferrini & Jeremy Vidal & Leah Sittenfeld & Jerome N. Feige & Pablo M. Garcia-Roves & , 2021. "Acute RyR1 Ca2+ leak enhances NADH-linked mitochondrial respiratory capacity," Nature Communications, Nature, vol. 12(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-27422-1
    DOI: 10.1038/s41467-021-27422-1
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-021-27422-1
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-021-27422-1?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Carles Cantó & Zachary Gerhart-Hines & Jerome N. Feige & Marie Lagouge & Lilia Noriega & Jill C. Milne & Peter J. Elliott & Pere Puigserver & Johan Auwerx, 2009. "AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity," Nature, Nature, vol. 458(7241), pages 1056-1060, April.
    2. Ran Zalk & Oliver B. Clarke & Amédée des Georges & Robert A. Grassucci & Steven Reiken & Filippo Mancia & Wayne A. Hendrickson & Joachim Frank & Andrew R. Marks, 2015. "Structure of a mammalian ryanodine receptor," Nature, Nature, vol. 517(7532), pages 44-49, January.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Su-Youn Cho & Young-Soo Chung & Hyoung-Ki Yoon & Hee-Tae Roh, 2022. "Impact of Exercise Intensity on Systemic Oxidative Stress, Inflammatory Responses, and Sirtuin Levels in Healthy Male Volunteers," IJERPH, MDPI, vol. 19(18), pages 1-9, September.
    2. Éverton Lopes Vogt & Maiza Cristina Von Dentz & Débora Santos Rocha & Jorge Felipe Argenta Model & Lucas Stahlhöfer Kowalewski & Samir Khal de Souza & Vitória de Oliveira Girelli & Paulo Ivo Homem de , 2021. "Metabolic and Molecular Subacute Effects of a Single Moderate-Intensity Exercise Bout, Performed in the Fasted State, in Obese Male Rats," IJERPH, MDPI, vol. 18(14), pages 1-17, July.
    3. Yi-Fang Cheng & Guang-Huar Young & Jiun-Tsai Lin & Hyun-Hwa Jang & Chin-Chen Chen & Jing-Yi Nong & Po-Ku Chen & Cheng-Yi Kuo & Shao-Hsuan Kao & Yao-Jen Liang & Han-Min Chen, 2015. "Activation of AMP-Activated Protein Kinase by Adenine Alleviates TNF-Alpha-Induced Inflammation in Human Umbilical Vein Endothelial Cells," PLOS ONE, Public Library of Science, vol. 10(11), pages 1-14, November.
    4. Aurore Claude-Taupin & Pierre Isnard & Alessia Bagattin & Nicolas Kuperwasser & Federica Roccio & Biagina Ruscica & Nicolas Goudin & Meriem Garfa-Traoré & Alice Regnier & Lisa Turinsky & Martine Burti, 2023. "The AMPK-Sirtuin 1-YAP axis is regulated by fluid flow intensity and controls autophagy flux in kidney epithelial cells," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
    5. Jia Luo & Changfa Tang & Xiaobin Chen & Zhanbing Ren & Honglin Qu & Rong Chen & Zhen Tong, 2020. "Impacts of Aerobic Exercise on Depression-Like Behaviors in Chronic Unpredictable Mild Stress Mice and Related Factors in the AMPK/PGC-1α Pathway," IJERPH, MDPI, vol. 17(6), pages 1-12, March.
    6. Yuanpei Li & Xiaoniu He & Xiao Lu & Zhicheng Gong & Qing Li & Lei Zhang & Ronghui Yang & Chengyi Wu & Jialiang Huang & Jiancheng Ding & Yaohui He & Wen Liu & Ceshi Chen & Bin Cao & Dawang Zhou & Yufen, 2022. "METTL3 acetylation impedes cancer metastasis via fine-tuning its nuclear and cytosolic functions," Nature Communications, Nature, vol. 13(1), pages 1-23, December.
    7. Weiwei Liu & Hao Zhou & Han Wang & Quanri Zhang & Renliang Zhang & Belinda Willard & Caini Liu & Zizhen Kang & Xiao Li & Xiaoxia Li, 2022. "IL-1R-IRAKM-Slc25a1 signaling axis reprograms lipogenesis in adipocytes to promote diet-induced obesity in mice," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    8. Yuqing Zhang & Shan Han & Congcong Liu & Yuanwen Zheng & Hao Li & Fei Gao & Yuehong Bian & Xin Liu & Hongbin Liu & Shourui Hu & Yuxuan Li & Zi-Jiang Chen & Shigang Zhao & Han Zhao, 2023. "THADA inhibition in mice protects against type 2 diabetes mellitus by improving pancreatic β-cell function and preserving β-cell mass," Nature Communications, Nature, vol. 14(1), pages 1-19, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-27422-1. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.